drugset / Trial / NCT01056289

Study Comparing Discontinuation Symptoms Of DVS SR In Subjects With Major Depressive Disorder (MDD)

NCT01056289

Phase 4 Completed 480 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Study Comparing Discontinuation Symptoms in subjects with Major Depressive Disorder treated for 24 Weeks with Open-label 50 mg Desvenlafaxine Succinate Sustained-Release Formulation (DVS SR)

Timeline

Start
2010-03
Primary completion
2011-02
Completion
2011-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator Desvenlafaxine Other / unclassified 25 mg Oral
Comparator Desvenlafaxine Other / unclassified 50 mg Oral